SISTEMA DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE DEHIDROEPIANDROSTERONA (DHEA) EN SUERO HUMANO
Mexico·Clase I·III. Agentes de diagnóstico·INOCHEM, S.A. DE
C.V.·Registered November 29, 2022- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- DEHYDROEPIANDROSTERONE (DHEA) ELISA
- Trade Name (English)
- DEHYDROEPIANDROSTERONE (DHEA) ELISA
- Analysis ID
- 1482R2022 SSA
- Registration Date
- November 29, 2022
- Name (Spanish)
- INOCHEM, S.A. DE C.V.
- Name (English)
- INOCHEM, S.A. DE C.V.
Access comprehensive regulatory information for SISTEMA DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE DEHIDROEPIANDROSTERONA (DHEA) EN SUERO HUMANO (SISTEMA DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE DEHIDROEPIANDROSTERONA (DHEA) EN SUERO HUMANO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1482R2022 SSA and manufactured by INOCHEM, S.A. DE C.V.. The device was registered on November 29, 2022.
This page provides complete registration details including product type (III. Agentes de diagnóstico), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.